Childhood malignant mesenchymoma

disease
On this page

Also known as malignant mesenchymomamalignant mesenchymoma of childhoodpaediatric malignant mesenchymomapediatric malignant mesenchymoma

Summary

Childhood malignant mesenchymoma (MONDO:0003691) is a disease and 5 clinical trials. Top therapeutic interventions include cyclophosphamide anhydrous, dactinomycin, and filgrastim. A subtype of malignant mesenchymoma — broader associated-gene and molecular evidence is on the parent page (see Disease family below).

At a glance

  • Clinical trials: 5

Clinical features

No curated clinical features (Orphanet) for this disease.

Identifiers

Disease identifiers

FieldValue
Canonical namechildhood malignant mesenchymoma
Mondo IDMONDO:0003691
DOIDDOID:5893
NCITC8097
UMLSC0279991
MedGen124688
Is cancer (heuristic)no

Also known as: childhood malignant mesenchymoma · malignant mesenchymoma · malignant mesenchymoma of childhood · paediatric malignant mesenchymoma · pediatric malignant mesenchymoma

Disease family

This is a subtype of malignant mesenchymoma. Genetic, therapeutic, and trial evidence is largely curated at the broader-term level — see the parent page for the associated-gene cohort and molecular evidence.

Classification path: disease › human disease › disease by etiologic mechanism › cancer or benign tumorneoplastic disease or syndromeneoplasmcancermalignant mesenchymomachildhood malignant mesenchymoma

Related subtypes (1): adult malignant mesenchymoma

Genetics & variants

GWAS landscape

No GWAS associations recorded — common-variant (GWAS) studies don’t cover this disease (typical for Mendelian / rare diseases). See the curated gene cohort and Mendelian overlap below.

Variant details and genetic-evidence tiers

No tiered GWAS variants or ClinVar records for this disease.

Genes & proteins

No associated-gene cohort resolved for this disease. Atlas builds the molecular and therapeutic sections — associated genes, protein families, druggability, pathways, interactions, and drug associations — by aggregating over a disease’s associated genes (resolved via GWAS / GenCC / ClinVar / CIViC), and none resolved here. This is expected for antibody-mediated, autoimmune, or otherwise non-gene-defined conditions; the curated evidence for this disease is its clinical features, GWAS susceptibility, and clinical trials (above).

Function

No pathway enrichment — requires an associated-gene cohort.

Therapeutics

No druggable-target or therapeutic data for this disease’s cohort.

Clinical trials & evidence

Clinical trials

Clinical trials: 5.

Phase distribution (across all retrieved trials)

PhaseTrials
PHASE32
Not specified2
PHASE11

Top trials by phase / activity

NCTPhaseStatusTitle
NCT00003958PHASE3COMPLETEDCombination Chemotherapy in Treating Patients With Previously Untreated Rhabdomyosarcoma
NCT00346164PHASE3COMPLETEDObservation, Radiation Therapy, Combination Chemotherapy, and/or Surgery in Treating Young Patients With Soft Tissue Sarcoma
NCT00720174PHASE1COMPLETEDCixutumumab and Doxorubicin Hydrochloride in Treating Patients With Unresectable, Locally Advanced, or Metastatic Soft Tissue Sarcoma
NCT04758325Not specifiedRECRUITINGThe Sarcoma Biology and Outcome Project
NCT01567046Not specifiedCOMPLETEDStudying Genes in Tissue Samples From Younger and Adolescent Patients With Soft Tissue Sarcomas

Drugs tested across these trials (top 30)

MoleculeMax phaseTrials referencing
CYCLOPHOSPHAMIDE ANHYDROUS41
DACTINOMYCIN41
FILGRASTIM41
IFOSFAMIDE41
SARGRAMOSTIM41
TOPOTECAN HYDROCHLORIDE41
VINCRISTINE SULFATE41
CIXUTUMUMAB21
CHEMBL474839101